“gke” Bowie-Dick-Simulation Test - Taiwan Registration bdca97736726f6a1c614f4d24e23dc3c
Access comprehensive regulatory information for “gke” Bowie-Dick-Simulation Test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bdca97736726f6a1c614f4d24e23dc3c and manufactured by gke-GmbH. The authorized representative in Taiwan is Yida Industrial Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
bdca97736726f6a1c614f4d24e23dc3c
Ministry of Health Medical Device Import No. 029005
DHA05602900507
Product Details
For details, it is Chinese approved copy of the imitation order
J General hospital and personal use equipment
J2800 Sterilization Process Indicator
Imported from abroad
Dates and Status
Nov 01, 2016
Nov 01, 2021